Senior Manager, Pharmacovigilance Agreements

Biogen

Research Triangle Park, NC, United States
Base: $134,000.00-$179,000.00; bonus/equity: cash ...
Safety data exchange agreements management
Cross-functional collaboration
Pharmacovigilance compliance and transparency
The Senior Manager collaborates with global stakeholders to ensure timely execution and maintenance of pharmacovigilance and safety data exchange agreements

Job Summary

  • The Senior Manager collaborates with global stakeholders to ensure timely execution and maintenance of pharmacovigilance and safety data exchange agreements.
  • Biogen offers a competitive compensation package including base salary, cash bonus, equity incentives, and a comprehensive benefits program supporting employees' physical, financial, emotional, and social well-being.
  • Biogen fosters an inclusive culture that values diverse backgrounds and perspectives, providing opportunities for learning, growth, and impactful contributions to life-changing medicines.

Matching Summary

The Senior Manager collaborates with global stakeholders to ensure timely execution and maintenance of pharmacovigilance and safety data exchange agreements.

Salary

Base: $134,000.00-$179,000.00; Bonus/Equity: Cash bonus and equity incentive opportunities; Benefits: Medical, Dental, Vision, Life insurance, wellness programs, paid time off, 401(k) with match, stock purchase plan, tuition reimbursement

Skills & Requirements

Must-have

  • Safety data exchange agreements management
  • Cross-functional collaboration
  • Pharmacovigilance compliance and transparency
  • Audit and inspection subject matter expertise
  • SDEA planning and execution
  • Strong communication and negotiation skills

Nice-to-have

  • Consensus building mindset
  • Continuous improvement focus
  • Project and document management skills
  • Ability to influence without authority
  • Building cross-functional relationships

Key Requirements

  • Bachelor’s degree in life sciences
  • 5 years industry experience in pharmacovigilance or GVP
  • Experience reviewing safety agreements or contracts
  • Familiarity with drug development lifecycle and regulations

Work Rights

Not specified

Tailored Resume

Cover Letter